{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MP2","FABP8","M-FABP"],"biotype":"protein_coding","hgnc_id":"HGNC:9117","gene_name":"peripheral myelin protein 2","omim_gene":["170715"],"alias_name":null,"gene_symbol":"PMP2","hgnc_symbol":"PMP2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:82352561-82359758","ensembl_id":"ENSG00000147588"}},"GRch38":{"90":{"location":"8:81440326-81447523","ensembl_id":"ENSG00000147588"}}},"hgnc_date_symbol_changed":"1992-11-10"},"entity_type":"gene","entity_name":"PMP2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","London North GLH"],"phenotypes":["Charcot-Marie-Tooth disease, demyelinating, type 1G, 618279"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}